CAS 63647-64-3

Benzenesulfonyl chloride, 4-[(trifluoromethyl)sulfonyl]-

Description:

Benzenesulfonyl chloride, 4-[(trifluoromethyl)sulfonyl]- is an organic compound characterized by the presence of both a sulfonyl chloride and a trifluoromethyl group attached to a benzene ring. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its reactivity, particularly due to the sulfonyl chloride functional group, which can undergo nucleophilic substitution reactions, making it useful in organic synthesis for the introduction of sulfonyl groups into various substrates. The trifluoromethyl group enhances the compound's electrophilicity and can influence its solubility and stability in different solvents. Additionally, this compound is often handled with caution due to its corrosive nature and potential to release toxic gases upon hydrolysis. Its applications span across pharmaceuticals, agrochemicals, and materials science, where it serves as an intermediate in the synthesis of more complex molecules. Proper safety measures should be observed when working with this substance due to its hazardous properties.

Formula: C₇H₄ClF₃O₄S₂

4-Trifluoromethanesulfonylbenzene-1-sulfonyl chloride

CAS: 63647-64-3

Versatile small molecule scaffold

Formula: C₇H₄ClF₃O₄S₂

Purity: Min. 95%

Molecular weight: 308.7 g/mol

Ref: 3D-NCA64764